Evidence map›Paper›PMID 31677030›Full record

ArticleMolecular and cellular biochemistry2020

SIRT3 promotes the invasion and metastasis of cervical cancer cells by regulating fatty acid synthase.

Li Xiu Xu, Li Jun Hao, Jun Qi Ma, Jing Kun Liu, Ayshamgul Hasim

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Targeting ferroptosis for precision medicine in cervical cancer.Apoptosis : an international journal on programmed cell death · 2025
    Review
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  7. Histone crotonylation in tumors (Review).Molecular and clinical oncology · 2025
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  9. The role of acetylation and deacetylation in cancer metabolism.Clinical and translational medicine · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Crotonylation modification and its role in diseases.Frontiers in molecular biosciences · 2024
    Review
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Li Xiu XuDepartment of Pathology, College of Basic Medicine, Medical University of Xinjiang, Ürümqi, People's Republic of China.
Li Jun HaoClinical Laboratory Center of People's Hospital, Xinjiang, People's Republic of China.
Jun Qi MaDepartment of Gynecology in the First Affiliated Hospital, Medical University of Xinjiang, Ürümqi, People's Republic of China.
Jing Kun LiuDepartment of Oncology, Cancer Center in the First Affiliated Hospital, Medical University of Xinjiang, Ürümqi, People's Republic of China.
Ayshamgul HasimDepartment of Pathology, College of Basic Medicine, Medical University of Xinjiang, Ürümqi, People's Republic of China. axiangu75@126.com.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNPeople's Hospital of Xinjiang Uygur Autonomous Region · CN

Funding

Program for Innovative Research Teams 99-11091107202The State Key Laboratory of Pathogenesis, Prevention, Treatment of High Incidence Diseases in Central Asia Fund SKL-HIDCA-2017-3Xinjiang Uygur Autonomous Region University Research Innovation Team Fund XJEDU2017T006
6 · The paper itself

Abstract

Sirtuin 3 (SIRT3) modulates mitochondria-localized processes and is implicated in the metabolic reprogramming of cancer cells, especially fatty acid (FA) synthesis. However, the relationship between SIRT3 and aberrant lipid synthesis in cervical cancer remains unclear. Here, we investigated the clinical relevance of SIRT3 expression in cervical squamous cell carcinoma (CSCC), cervical intraepithelial neoplasia (CIN), and normal tissues. To analyze the role of SIRT3 in CCSC in vitro, endogenous SIRT3 levels were up- and down-regulated in SiHa and C33a cells, respectively, via lentiviral-based transfection. Levels were quantified using qRT-PCR. Acetylation levels for acetyl-coA carboxylase (ACC1) were measured with the anti-acetyllysine antibody. Knockdown of SIRT3 reduced levels of cellular lipid content in cells. To investigate the role of SIRT3 in cell proliferation, nude mice were xenografted with SIRT3-overexpressing or SIRT3-knockdown CCSC cells. Overall, the results demonstrate that SIRT3 significantly contributed to the reprogramming of FA synthesis in CCSC by up-regulating ACC1 to promote de novo lipogenesis by SIRT3 deacetylation. Moreover, the findings show that the SIRT3-mediated regulation of FA synthesis played a critical role in the proliferation and metastasis of CCSC cells, suggesting that SIRT3 has therapeutic potential in CCSC treatment.

Indexed as

AnimalsCarcinoma, Squamous CellCell Line, TumorFatty AcidsFatty Acid Synthase, Type IFemaleHumansMiceMice, NudeNeoplasm InvasivenessNeoplasm MetastasisNeoplasm ProteinsSirtuin 3Uterine Cervical NeoplasmsFASN protein, humanFatty AcidsFatty Acid Synthase, Type INeoplasm ProteinsSIRT3 protein, humanSirtuin 3ACC1Cervical carcinomaFatty acid synthesisSIRT3

Identifiers

PMID31677030
OpenAlexW2982759283

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.